AANMELDEN INLOGGEN
      • Locatie
      • RAI
      • Amsterdam, Europaplein, Amsterdam, Netherlands
      • 1078 GZ Amsterdam
      • Noord-Holland, Nederland
      • Van
      • 29 november 2016
      • Tot
      • 30 november 2016
    • Algemene informatie

      • Leeftijdscategorie
      • alle leeftijden
        • Indicatie entreeprijzen
        • - volwassen
        • - kinderen
        • - senioren / 65+
        • 0,00
        • 2899,00
        • € 0,00
      • (Openings)tijden
      • 09:00 - 16:00 uur

      Extra informatie

      Learn and benchmark with attendees from the main cell, gene and immunotherapy communities.

      Optimise your process, manufacturing capabilities and analytical strategies:

      - How do you deal with the challenge of CMO selection, process transfer, and demonstration of comparability?
      - What are the requirements for the commercial manufacturing process?
      - What other steps must be taken in order to launch large scale manufacturing?
      - What is best practise for defining the efficacy of your product?
      - How do you correlate raw material attributes to your cells?
      - What is best practise for assessing critical raw materials?

      Ensure stringent cold chain and process automation strategies:

      - How do you develop a stringent, commercially viable manufacturing strategy?
      - How do you bring bioprocessing technologies to these therapies to allow them to be made for the masses?
      - What is best practise for keeping costs down in scale-out systems?
      - How do you design facilities to make them financially feasible?
      - What is best practise when working with automated systems for bioreactors?
      - What are the major questions and issues surrounding cryopreservation?

      Learn how to accelerate preclinical studies and push products into the clinic:

      - Which new applications are showing the biggest promise for the clinic?
      - What is needed from preclinical studies so a product can move smoothly into the clinic?
      How do you apply risk based approaches to reduce the amount of data required?
      - How can the results from preclinical animal models be used to convince investors that your product is worthwhile?
      - What is the best way to set CQA's early on in your process?
      - How have companies secured funding for preclinical studies?

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